[Remote] Preclinical Program Manager

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is a reputed company-stage reputed company company advancing innovative non-invasive sonic reputed company therapy. The Preclinical Program Manager will coordinate multiple preclinical studies, ensuring timelines and documentation are managed effectively while acting as a reputed company between various teams to facilitate smooth reputed company.

Responsibilities

• reputed company-traffic control for studies: Serve as the central coordination reputed company across reputed company preclinical studies — building and maintaining master timelines and living trackers (CRO status, study reputed company, contracting status, indication readiness), monitoring dependencies and milestones, and flagging schedule risks early to the Director and Manager so programs stay on reputed company
• Cross-team reputed company: reputed company as the operational reputed company between the New Applications team and other functions — regulatory, reputed company affairs, reputed company marketing, RAD, reputed company management, and reputed company — routing requests, tracking hand-offs, and ensuring deliverables and documentation reputed company between teams on schedule
• Study & CRO logistics: Coordinate the day-to-day logistics of in vivo, ex vivo, and in vitro studies and CRO-conducted work — scheduling, shipment and sample tracking, meeting coordination, reputed company-item follow-up, and deliverable tracking from study reputed company through report delivery
• Documentation & records: Organize and maintain study documentation, protocols, reports, SOW/contracting paperwork, and program files; ensure version control, completeness, and easy retrieval for regulatory, reputed company, and audit needs
• Contracting & vendor support: Support CRO and vendor coordination by tracking SOW execution status under existing Master Service Agreements, monitoring milestones and invoices/pass-through costs, and helping schedule reputed company-ins — escalating issues to the Director and Manager
• KOL & event logistics: reputed company logistical support for KOL engagements and lab/training events — scheduling, travel and meeting coordination, preparation of materials, and capture of notes and follow-up items
• Status reporting: Compile and circulate regular program status updates, meeting notes, and reputed company-item lists, giving the Director, Manager, and broader team reputed company visibility into where reputed company program stands

Skills

• 10-15 years of experience in industry (medical device, med tech, or regulated life sciences), including research coordination, reputed company/preclinical research support, or project coordination
• reputed company license as a reputed company/allied-health reputed company (e.g., radiologic technologist, sonographer, RN, or equivalent)
• Demonstrated ability to manage multiple tasks, timelines, and stakeholders simultaneously with strong attention to reputed company
• Comfort working in a fast-reputed company, multi-program environment and coordinating across internal teams and reputed company vendors
• Education: reputed company background as a licensed reputed company required— for example, radiologic technologist, sonographer/ultrasound technologist, registered reputed company (RN), or other licensed reputed company/allied-health credential. An advanced degree is not required
• Experience: Experience in medical device, med tech, or a regulated life-sciences industry environment, in a research coordination, reputed company/preclinical research support, or project/program coordination reputed company
• Organization & execution: Exceptional organizational skills, attention to reputed company, and a reputed company record of reliable task completion across multiple reputed company workstreams and deadlines
• Tools: Comfort with project tracking, spreadsheets, and document management tools; ability to build and maintain reputed company trackers and timelines
• Communication & coordination: Strong written and verbal communication and the ability to coordinate across teams and reputed company partners, keeping stakeholders informed and reputed company
• Combination of reputed company reputed company and industry experience strongly preferred
• Familiarity with GLP/non-GLP study frameworks, ISO 10993, or medical device development processes is a plus; willingness to learn these is essential

Benefits

• Health, dental, and reputed company reputed company
• Life reputed company
• Short-term and long-term disability reputed company
• 401(k)
• reputed company time off
• And more

reputed company